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Past Experience

  • Clinical Research Associate (CRA) Belgium
    August 2015 --- August 2016

    Mainly working on immune oncology phase II and phase III clinical trials. 

    experience in start up phase, initiation, monitoring, close out visits. 

  • Clinical Research Associate (CRA) Belgium
    July 2011 --- August 2015

    Mainly working on oncology phase II and phase III clinical trials. 

    experience in start up phase, initiation, monitoring, close out visits. 

  • Clinical Research Coordinator Belgium
    May 2010 --- April 2011

    Coordinating the vaccines supply intended for the clinical trials.

  • clinical project assistant Belgium
    April 2007 --- May 2010

    IVRS Project Assistant. 

  • Research Assistant Belgium
    September 2004 --- June 2005

    overseeing students' practical classes (use of softwares and work in



Self Assessment :
Result OrientedAdaptabilityAnalytical thinkingAssertivenessAttention to detailAuthenticityCollaborationCommunicativeCoordinationCuriosityEfficiencyFlexibilityIndependenceInterest in knowledgeOrganizationProactivityProblem solvingResiliencyResponsibilitySelf-confidenceSelf-disciplineService orientedSociabilityTrustWillingness to compromiseOptimism


Self Assessment :
NegotiationCancer ResearchCAPAClinical monitoringClinical operationsClinical researchClinical trial audits and inspectionsClinical trial managementClinical Trial Management System (CTMS)Clinical trialsCommunication SkillsComplianceContract negotiationCRFCROCTMSCustomer ServiceData cleaningData entryData ManagementDrug Supply Management activitieseCRFEDCEfficacy trialsElectronic Data Capture (EDC) EnglishEthics submission and approval processGood Clinical Practice (GCP)Healthcare industryInformed Consent DocumentsInformed Consent ProcessIVRSLife SciencesMicrosoft OfficeOncology Clinical Researchpeople managementProblem SolvingTime Management

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Build and manage the Trial Master File (TMF) Interpret data Monitor a clinical study Use content management systemsAssist study siteAssist with site trainingAttend seminars, courses and meetings within and outside the companyCoach clinical staffCollaborate with principal investigatorCollaborate with project teamCommunicate with investigatorCommunicate effectively on different company levelsInformed consent processInitiate clinical trials Interact with CROsInteract with ethics committeeInteract with KOLInteract with nursesInteract with pharmacistsInteract with physicians


  • Master in Bioengineering from UCL in 2004

Training and Certification

  • Clinical Project Manager in 2016 Training
  • Senior Clinical Research Associate in 2016 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    Full Proficiency
    Full Proficiency
    Elementary Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Project Manager (CPM)
  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    BrightOwl freelancer :    40 Hours per week :    100% Free Per Month(in coming months)
  • International:

Area / Region

Brussels, Belgium


Driving License
  • Yes